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Indole-3-carboxaldehyde - 97%, high purity , CAS No.487-89-8

    Grade & Purity:
  • ≥97%
In stock
Item Number
I106884
Grouped product items
SKU Size
Availability
Price Qty
I106884-5g
5g
9
$25.90
I106884-10g
10g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$46.90
I106884-25g
25g
4
$68.90
I106884-100g
100g
3
$246.90
I106884-500g
500g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$1,108.90

Basic Description

Synonyms indole 3-carboxaldehyde | 1H-indole-3-aldehyde | CU-00000000108-1 | I0027 | AB00443651-03 | A-Indolylaldehyde | Q27103575 | .beta.-Indolylaldehyde | AM1029 | C08493 | CHEBI:28238 | Indol-3-carbaldehyd | AC-23425 | AG-205/01412034 | 3-Formylindol | A7354 |
Specifications & Purity ≥97%
Storage Temp Argon charged
Shipped In Normal

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organoheterocyclic compounds
Class Indoles and derivatives
Subclass Indoles
Intermediate Tree Nodes Not available
Direct Parent Indoles
Alternative Parents Aryl-aldehydes  Substituted pyrroles  Benzenoids  Vinylogous amides  Heteroaromatic compounds  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular Framework Aromatic heteropolycyclic compounds
Substituents Indole - Aryl-aldehyde - Substituted pyrrole - Benzenoid - Pyrrole - Heteroaromatic compound - Vinylogous amide - Azacycle - Aldehyde - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound
Description This compound belongs to the class of organic compounds known as indoles. These are compounds containing an indole moiety, which consists of pyrrole ring fused to benzene to form 2,3-benzopyrrole.
External Descriptors an indole-phytolexin

Associated Targets(Human)

DHFR Tclin Dihydrofolate reductase (3072 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
IMPDH2 Tclin Inosine-5'-monophosphate dehydrogenase 2 (1326 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TYR Tclin Tyrosinase (717 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ALOX15 Tchem Arachidonate 15-lipoxygenase (7108 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CYP2A6 Tchem Cytochrome P450 2A6 (2861 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
BGC-823 (3035 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HCT-8 (3484 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
MCF7 (126967 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
A549 (127892 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Bel-7402 (4577 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HeLa (62764 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
MDA-MB-231 (73002 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
KETR3 (279 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
NR4A2 Tchem Nuclear receptor subfamily 4 group A member 2 (460 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HeLa S3 (477 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Pseudomonas aeruginosa (123386 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Klebsiella pneumoniae (43867 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Acinetobacter baumannii (41033 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Escherichia coli (133304 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Phytophthora infestans (820 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Phytophthora capsici (336 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Rhizomucor miehei (120 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Penicillium chrysogenum (1593 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Cryptococcus neoformans (21258 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Candida albicans (78123 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Meloidogyne incognita (862 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mus musculus (284745 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Human alphaherpesvirus 1 (11089 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Human immunodeficiency virus 1 (70413 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Paecilomyces variotii (130 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
L5178Y (1809 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
PTR1 Pteridine reductase 1 (345 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TUBB2B Tubulin (2175 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Cryphonectria parasitica (24 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

Pubchem Sid 488181098
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488181098
IUPAC Name 1H-indole-3-carbaldehyde
INCHI InChI=1S/C9H7NO/c11-6-7-5-10-9-4-2-1-3-8(7)9/h1-6,10H
InChIKey OLNJUISKUQQNIM-UHFFFAOYSA-N
Smiles C1=CC=C2C(=C1)C(=CN2)C=O
Isomeric SMILES C1=CC=C2C(=C1)C(=CN2)C=O
WGK Germany 3
RTECS NL5993600
Molecular Weight 145.16
Beilstein 21313
Reaxy-Rn 114117
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=114117&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

23 results found

Lot Number Certificate Type Date Item
L2206654 Certificate of Analysis Apr 18, 2025 I106884
A2316033 Certificate of Analysis Mar 10, 2025 I106884
B2518028 Certificate of Analysis Feb 21, 2025 I106884
L2206657 Certificate of Analysis Feb 17, 2025 I106884
L2206633 Certificate of Analysis Sep 13, 2024 I106884
L2206631 Certificate of Analysis Sep 13, 2024 I106884
L2206630 Certificate of Analysis Sep 13, 2024 I106884
L2206655 Certificate of Analysis Sep 13, 2024 I106884
L2206634 Certificate of Analysis Sep 13, 2024 I106884
K2408435 Certificate of Analysis Jul 01, 2024 I106884
K2408436 Certificate of Analysis Jul 01, 2024 I106884
K2408434 Certificate of Analysis Jul 01, 2024 I106884
I2102243 Certificate of Analysis Jun 06, 2023 I106884
I2102244 Certificate of Analysis Jun 06, 2023 I106884
J2422046 Certificate of Analysis Jun 06, 2023 I106884
I2102245 Certificate of Analysis Jun 06, 2023 I106884
I2102246 Certificate of Analysis Jun 06, 2023 I106884
F2124234 Certificate of Analysis Mar 16, 2023 I106884
F2124235 Certificate of Analysis Mar 16, 2023 I106884
C2405062 Certificate of Analysis Nov 22, 2022 I106884
G2311057 Certificate of Analysis Nov 22, 2022 I106884
L2206656 Certificate of Analysis Nov 22, 2022 I106884
G2021117 Certificate of Analysis May 07, 2022 I106884

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Chemical and Physical Properties

Solubility Insoluble in water.
Sensitivity Air sensitive
Flash Point(°C) 240℃
Melt Point(°C) 193-198°C
Molecular Weight 145.160 g/mol
XLogP3 1.700
Hydrogen Bond Donor Count 1
Hydrogen Bond Acceptor Count 1
Rotatable Bond Count 1
Exact Mass 145.053 Da
Monoisotopic Mass 145.053 Da
Topological Polar Surface Area 32.900 Ų
Heavy Atom Count 11
Formal Charge 0
Complexity 158.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Citations of This Product

1. Haiyan Zhao, Hongfu He, Zhongjie Shen, Chunle Wei, Limin Yin, Yunying Zhu, Hongxia Lu, Runjiang Song, Deyu Hu.  (2023)  Development and Mechanism Investigation of Novel Thioacetalized Indoles as Antiphytoviral Agents.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,     
2. Lingling Ma, Lv Li, Minghao Yuan, Lei Bai, Anran Zhang, Xiaoming Yan, Gaohong He, Fengxiang Zhang.  (2022)  Hydrophilic–Hydrophobic Bulky Units Modified Anion Exchange Membranes for Fuel Cell Application.  ACS Sustainable Chemistry & Engineering,  10  (18): (5748–5757). 
3. Xiang He, Ruyue Liu, Huiqing Liu, Ruixiao Wang, Zhenhao Xi, Yixiang Lin, Jie Wang.  (2021)  Facile Preparation of Tunicate-Inspired Chitosan Hydrogel Adhesive with Self-Healing and Antibacterial Properties.  Polymers,  13  (24): (4322). 
4. Jia Yin, Yujie Song, Yaozhong Hu, Yuanyifei Wang, Bowei Zhang, Jin Wang, Xuemeng Ji, Shuo Wang.  (2021)  Dose-Dependent Beneficial Effects of Tryptophan and Its Derived Metabolites on Akkermansia In Vitro: A Preliminary Prospective Study.  Microorganisms,  (7): (1511). 
5. Xiaona Zhang, Liang Sun, Wei Zheng, Xichang Bao, Ning Wang, Ting Wang, Renqiang Yang.  (2013)  The preparation and properties of bulk-heterojunction organic solar cells with indole-containing fulleropyrrolidine derivatives as acceptors.  TETRAHEDRON,  69  (9544). 
6. Yewei Xu, Haoran Zhu, Shijie Mo, Yangqing Mao, Chi Zhong, Ying Huang, Rui Yuan, Min Zheng, Mingru Zhou, Guanjun Chang.  (2024)  Adsorption of 2,4,6-trinitrotoluene by indole-based porous organic polymer with suitable three-dimensional space size via physisorption and chemisorption.  POLYMER,  300  (126993). 
7. Han Ziyi, Fu Jian, Gong Aiyan, Ren Wenkai.  (2025)  Bacterial indole-3-propionic acid inhibits macrophage IL-1β production through targeting methionine metabolism.  Science China-Life Sciences,    (1-14). 
8. Zhang Junzhi, Lin Binyan, Zhang Ying, Hu Xiaochao, Liu Tongtong, Liu E-Hu, Liu Shijia.  (2024)  Baitouweng decoction alleviates ulcerative colitis by regulating tryptophan metabolism through DOPA decarboxylase promotion.  Frontiers in Pharmacology,  15   
9. Susu Zhao, Lixin Sun, Yibo Liu, Chuanhui Gao, Li Ding, Ze Kan, Yuetao Liu.  (2025)  Cation-indole supramolecular interaction constructed novel silicone anti-fouling materials.  CHEMICAL ENGINEERING JOURNAL,  505  (159423). 
10. Mengshi Xiao, Jiayuan Bi, Xinmiao Ren, Xiaodan Fu, Dongyu Li, Rong Li, Haijin Mou.  (2024)  Evaluation of potential prebiotic activity of a novel fucose-containing trisaccharide prepared from bacterial exopolysaccharides.  Food Bioscience,  60  (104380). 
11. Jia Cheng Qian, Heng Peng Zhang, Yi Wang, Dan Liu.  (2024)  Heating conversion of indole-3-carbinol into N-substituted oligomers with anti-melanoma effect.  Food Chemistry-X,  22  (101410). 
12. Yufei Deng, Xiaoying Hou, Qian Fang, Haiping Wang, Xiaoxuan Li, Zhiyong Hu, Zhaolu Liu, Limei Fan, Yunyi Liu, Zhengqi Fu, Xiji Shu, Binlian Sun, Lijun Huang, Yuchen Liu.  (2025)  High-salt diet decreases FOLFOX efficacy via gut bacterial tryptophan metabolism in colorectal cancer.  MOLECULAR MEDICINE,  31  (66). 
13. Yvhao Xie, Xinxin Li, Qingshi Meng, Jinjun Li, Xin Wang, Liying Zhu, Weiwei Wang, Xiaoqiong Li.  (2024)  Interplay between gut microbiota and tryptophan metabolism in type 2 diabetic mice treated with metformin.  Microbiology Spectrum,     
14. Yating Xu, Li Ning, Yu Si, Xiu Li, Ruyue Wang, Qingling Ren.  (2025)  Metformin-mediated intestinal AMPK activation ameliorates PCOS through gut microbiota modulation and metabolic pathways.  Frontiers in Endocrinology,  16   
15. Xiaomeng Chu, Zeqiang Liu, He Gao, Kang Geng, Shaojie Liu, Xuteng Xing, Erjun Tang, Nanwen Li, Song Zhao.  (2024)  Promising candidates of ether-free backbone comb-shaped sulfonated poly(oxindole biphenylene) membranes for enhanced electrochemical hydrogen compression performance.  JOURNAL OF MEMBRANE SCIENCE,  698  (122626). 

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